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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723878Generated: November 2, 2026

Water → 4-(4-Methylpiperazin-1-yl)butanenitrile

https://huagongshe.com/reaction/1723878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromobutyronitrileHCID 21412—
Reactant1-MethylpiperazineHCID 53167—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-(4-Methylpiperazin-1-yl)butanenitrileHCID 18626390—

Reaction Steps

In a 25 mL flask was placed 1-methyl-piperazine (0.52 g, 5.1 mmol), 4-bromobutyronitrile (0.78 g, 5.3 mmol) and potassium carbonate (0.71 g, 5.3 mmol) suspended in acetonitrile (5 mL). The reaction mixture was stirred at rt for 4 h., followed by addition of H2O (20 mL) and extraction with ethyl acetate (3×25 mL). The combined organic phases were washed with brine (25 mL), dried (MgSO4) and evaporated to dryness to produce 0.72 g of crude 14 which was used without further purification in the synthesis of compound 15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485651B2
Source datasetuspto-grants-2009_02
ORD IDord-5c6b877b0d2a4cf9a6061b9a87d1ae72
Source noteuspto-grants-2009_02